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Completed

NCT Number: NCT04639492

Postbiotic MBS and Metformin Combination in Patients With T2DM

The primary objective is to evaluate the effect of MBS treatment in human subjects, and to validate its impact on intestinal flora and diabetes symptoms on diabetic patients undertaking metformin. The scientific data collected will be referenced for future product development.

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Key information

Age range

20 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Microbio Investigative Site

Taipei, 106, Taiwan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female subject who aged from 20 to 70.
  • BMI in between 18.5 and 35 kg/m2 inclusively.
  • Fasting blood sugar ≥ 126 mg/dL, and confirmed diagnosis of type-II diabetes.
  • 30 days prior to the screening visit (V1), HbA1c is steadily maintained in between 7-10% by medication.
  • Prior to the screening visit (V1), subjects have been regularly taken 500-200 mg/day for at least 90 days.

Exclusion criteria

  • Pregnant or breastfeeding women or female subjects plan to enter pregnancy during study period.
  • Subjects who are allergic to soy or products containing it.
  • At investigator's discretion, subjects are unlikely to comply with study procedures due to a history of alcohol or drug addiction.
  • Subjects on vegetarian diet or other special diets (eg. Ketogenic or gluten-free diets).
  • Subjects have ongoing participation in another clinical trial that involves the use of investigational drugs, medical devices, dietary supplements, and/or cosmetics.
  • Subject with impaired renal function confirmed by Serum Total Bilirubin ≥ 1.5 upper limit of normal [ULN], Aspartate Transaminase/ Alanine Transaminase (AST/ALT) ≥ 2 ULN, Creatinine ≥ 2 ULN or eGFR <60 mL/min/1.73 m^2.
  • Subjects who have been diagnosed with malignant tumors within five (5) years before the screening visit (V1) with exception to subjects with topical cancer but show significant recovery following investigator's assessment, such as basal or squamous cell skin cancer, superficial bladder cancer, or prostate or cervix or carcinoma in situ of the breast.
  • 30 days prior to screening visit (V1), subjects have taken antibiotics, synthetic drugs (Sulfonamides, Fluoroquinolone, etc.), anti-fungal or anti-viral medication but not limited to topical forms for use in skin application.
  • Within 14 days prior to screening visit (V1), subjects have taken products or supplements that contain probiotics or prebiotics.
  • Within 14 days prior to screening visit (V1), subjects experience diarrhea caused by gastrointestinal infection (3 times of watery stool within 24 hours).
  • Within14 days prior to screening visit (V1), subjects have taken steroids, immunosuppressant, and/or inflammatory medicines.
  • Subjects took or intend to take medications other than metformin that may affect intestinal flora within 30 days prior to screening visit, during screening period or whole trial period. Examples of this kind of medication include DPP-4 inhibitors, GLP-1 receptor agonists, acarbose, hypoglycemic sulfonamides, thiazolidinediones, SGLT2 inhibitors, and insulin.

Treatment and study plan

MBS oral solution

Dietary Supplement

Oral BIDAC, twice a day before breakfast and dinner times

Primary outcomes

  1. Post-treatment changes of intestinal flora

    Time frame: 4, 8,12 weeks post-treatment

    Post-treatment changes from baseline in microbial composition, abundance, variation of subject's intestinal flora at 4, 8, 12 weeks.

Secondary outcomes

  1. Post-treatment changes from baseline in fasting plasma glucose at 12 weeks

    Time frame: 12 weeks post-treatment

  2. Post-treatment changes from baseline in HbA1c at 12 weeks

    Time frame: 12 weeks post-treatment

  3. Post-treatment changes from baseline in HOMA-IR at 12 weeks

    Time frame: 12 weeks post-treatment

  4. Post-treatment changes from baseline in blood lipids composition at 12 weeks

    Time frame: 12 weeks post-treatment

    Changes of triglyceride, high-density lipoprotein (HDL), and low-density lipoprotein (LDL)

  5. Post-treatment changes from baseline in immune factors at 12 weeks

    Time frame: 12 weeks post-treatment

    Changes of CRP, IL6, TNF-α expression

  6. Incidence of treatment-emergent adverse events(TEAE)

    Time frame: 12 weeks post-treatment

Sponsors and collaborators

Lead sponsor

Microbio Co Ltd

Industry

Registry information

Official study title

Evaluating the Effect and Safety of Postbiotic MBS and Metformin Combination on Gut Microbiota and Symptom in Patients With Diabetes

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Nov 20, 2020
Registry last updated
Jan 5, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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